Unlock Autism

Although in it’s too early, this Autism Fever and the Brain research is very promising and holds a lot of hope for Autism sufferers.

ScienceDaily (Apr. 2, 2009) – Scientists at Albert Einstein College of Medicine of Yeshiva University have proposed a sweeping new theory of autism that suggests that the brains of people with autism are structurally normal but dysregulated, meaning symptoms of the disorder might be reversible.

The central tenet of the theory, published in the March issue of Brain Research Reviews, is that autism is a developmental disorder caused by impaired regulation of the locus coeruleus, a bundle of neurons in the brain stem that processes sensory signals from all areas of the body.

The new theory stems from decades of anecdotal observations that some autistic children seem to improve when they have a fever, only to regress when the fever ebbs. A 2007 study in the journal Pediatrics took a more rigorous look at fever and autism, observing autistic children during and after fever episodes and comparing their behavior with autistic children who didn’t have fevers. This study documented that autistic children experience behavior changes during fever.

“On a positive note, we are talking about a brain region that is not irrevocably altered. It gives us hope that, with novel therapies, we will eventually be able to help people with autism,” says theory co-author Mark F. Mehler, M.D., chairman of neurology and director of the Institute for Brain Disorders and Neural Regeneration at Einstein.

Autism is a complex developmental disability that affects a person’s ability to communicate and interact with others. It usually appears during the first three years of life. Autism is called a “spectrum disorder” since it affects individuals differently and to varying degrees. It is estimated that one in every 150 American children has some degree of autism.

Einstein researchers contend that scientific evidence directly points to the locus coeruleus-noradrenergic (LC-NA) system as being involved in autism. “The LC-NA system is the only brain system involved both in producing fever and controlling behavior,” says co-author Dominick P. Purpura, M.D., dean emeritus and distinguished professor of neuroscience at Einstein.

The locus coeruleus has widespread connections to brain regions that process sensory information. It secretes most of the brain’s noradrenaline, a neurotransmitter that plays a key role in arousal mechanisms, such as the “fight or flight” response. It is also involved in a variety of complex behaviors, such as attentional focusing (the ability to concentrate attention on environmental cues relevant to the task in hand, or to switch attention from one task to another). Poor attentional focusing is a defining characteristic of autism.

“What is unique about the locus coeruleus is that it activates almost all higher-order brain centers that are involved in complex cognitive tasks,” says Dr. Mehler.

Drs. Purpura and Mehler hypothesize that in autism, the LC-NA system is dysregulated by the interplay of environment, genetic, and epigenetic factors (chemical substances both within as well as outside the genome that regulate the expression of genes). They believe that stress plays a central role in dysregulation of the LC-NA system, especially in the latter stages of prenatal development when the fetal brain is particularly vulnerable.

As evidence, the researchers point to a 2008 study, published in the Journal of Autism and Developmental Disorders, that found a higher incidence of autism among children whose mothers had been exposed to hurricanes and tropical storms during pregnancy. Maternal exposure to severe storms at mid-gestation resulted in the highest prevalence of autism.

Drs. Purpura and Mehler believe that, in autistic children, fever stimulates the LC-NA system, temporarily restoring its normal regulatory function. “This could not happen if autism was caused by a lesion or some structural abnormality of the brain,” says Dr. Purpura.

“This gives us hope that we will eventually be able to do something for people with autism,” he adds.

The researchers do not advocate fever therapy (fever induced by artificial means), which would be an overly broad, and perhaps even dangerous, remedy. Instead, they say, the future of autism treatment probably lies in drugs that selectively target certain types of noradrenergic brain receptors or, more likely, in epigenetic therapies targeting genes of the LC-NA system.

“If the locus coeruleus is impaired in autism, it is probably because tens or hundreds, maybe even thousands, of genes are dysregulated in subtle and complex ways,” says Dr. Mehler. “The only way you can reverse this process is with epigenetic therapies, which, we are beginning to learn, have the ability to coordinate very large integrated gene networks.”

“The message here is one of hope but also one of caution,” Dr. Mehler adds. “You can’t take a complex neuropsychiatric disease that has escaped our understanding for 50 years and in one fell swoop have a therapy that is going to reverse it – that’s folly. On the other hand, we now have clues to the neurobiology, the genetics, and the epigenetics of autism. To move forward, we need to invest more money in basic science to look at the genome and the epigenome in a more focused way.”

Science Daily is an excellent site for Autism related research, support them so they can support us..

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Can leaching plastics be involved with the rise in Autism? In m y view ABSOLUTELY! These days everything which was once housed in glass is now in plastic. Plastic water bottles embossed with company logo’s straight from the  capital of lead poisining – China, fill almost every corporate portfolio of chatzke giveaways. Its time to rid ourselves of plastics and go back to glass. Rep Charles Schumer of NY has just recently proposed a ban of BPA’s in any baby product, at least someone is aware and doing something about it!
BPA or Bisphenol A is Everywhere – Are We Safe?
BPA otherwise known as Bisphenol A is a compound widely used in the manufacture of plastics and epoxy resins. This
industrial chemical has created quite a stir since 2007 and is still a subject of intense controversy. BPA can be found
in plastics around us and is in the products that we use every day, from DVDs to eyeglasses to mobile phones.
Normally, BPA is harmless, that is, until it gets in contact with food and drinks and leaches out. According to
a report of the National Toxicology Program (NTP) of the U.S. National Institutes of Health (NIH), “the primary
source of exposure to BPA for most people is through the diet…BPA in food and beverages accounts for the majority
of daily human exposure.”

However, not all plastics contain BPA. Plastics are categorized into 7 types according to the recycling process
and the classification codes are located at the bottom of plastic containers. According to NTP, only plastic no. 7,
designated as “other” contains BPA. Incidentally there are other organizations which report that BPA is also found in
plastic no. 3.

Some of the adverse effects that BPA may cause include the following:

BPA is an endocrine disrupting chemical (EDC) that mimics the neurotoxic properties of the hormone estrogen.
According to the Pediatric Environmental Health Specialty Unit (PEHSU) of the Association of Occupational and
Environmental Clinics (AOEC). “BPA has been associated with increases in developmental disorders of the brain and
nervous system in animals. These developmental disorders in animals are like problems such as ADHD (attention deficit
hyper-reactivity disorder) in humans.”

PEHSU reports that “BPA may cause changes in cells in breasts, the uterus, and the prostate which can increase
risk of cancers.” The September 2008 report of NTP suggests that BPA exposure may be linked to prostate and brain
cancer.

The NTP report also says that BPA can cause behavioral problems in fetuses, infants and children. It can induce
early onset of puberty in girls and can cause reproductive disorders.

High BPA levels have been linked to increased risk for cardiovascular disease and diabetes.

It comes as no surprise that these findings have generated a strong anti-BPA movement worldwide. To understand the
controversy behind BPA, let’s look at some of the events that have occurred in the last two years.

March 2007. A class action lawsuit was filed against baby bottle manufacturers on behalf of Californian babies who
may have been adversely affected by BPA.

November 2007. Researchers from the University of Cincinnati published an article in Toxicology Letters
(online edition) reporting that BPA is leaching out of the polycarbonate bottles popularly used as drinking bottles.
This report led to Nalgene plastic bottles taken off the shelves in Canada.

The Environmental Working Group (EWG) tested infant formulas for BPA and detected BPA in some of the most
popular brands. When questioned, 4 out of the top 5 companies admitted using BPA in their packaging.

January 2008. The National Center for Environmental Health of the Centers for Disease Control and Prevention (CDC)
published a paper which reported that BPA was detected in the urine of 92.6% of 2,517 participants during the
2003-2004 National Health and Nutrition Examination Survey (NHNES).

April 2008. Canada announced its plans to ban
BPA-containing bottles. The US FDA established an
agency-wide BPA task force to facilitate cross-agency
review of current research and new information on BPA for
all FDA regulated products.

May 2008. In a health call, “leaders of the Committee on
Energy and Commerce threatened to subpoena the Food and
Drug Administration (FDA) for records the agency used in
determining that the chemical bisphenol A (BPA) was safe
for use in making infant formula liners and other products
intended for infants and children”, according to a report
in the Journal of the American Medical Association (JAMA).

July 2008. The European Food Safety Authority’s AFC Panel
declared that human exposure to BPA is too low to cause any
real harm. According to the panel’s report, the human body
rapidly metabolises and eliminates BPA out of the body.
September 3, 2008

The National Toxicology Program (NTP) issued a report on
BPA, expressing the following concerns: – “some concern”
for effects on the brain, behavior, and prostate gland in
fetuses, infants, and children at current human exposures
to BPA. – “minimal concern” for effects on the mammary
gland and an earlier age for puberty for females, in
fetuses, infants, and children at current human exposures
to BPA. – “negligible concern” that exposure of pregnant
women to BPA will result in fetal or neonatal mortality,
birth defects, or reduced birth weight and growth in their
offspring. – “negligible concern” that exposure to BPA will
cause reproductive effects in non-occupationally exposed
adults and “minimal concern” for workers exposed to higher
levels – in occupational settings. “Some concern”
represents a midpoint in a 5-point scale of concern, with
“serious concern” as the highest and “negligible concern”
as the lowest.

September 2008. Researchers at the University of Exeter
(UK) re-examined the previously mentioned NHNES BPA urine
data. They found that high levels of BPA in the urine were
associated with chronic diseases such as cardiovascular
disorders, diabetes, and kidney problems. The BPA
Subcommittee of the Science Board to the US FDA met on
September 16, 2008 to discuss BPA assessment.

October 2008. Two studies reported research results in mice
exposed to BPA. One study reported that pregnant mice
exposed to BPA suffered from altered the cellular structure
of the breasts. A second study showed that female mice’s
exposure to low-dose BPA during fetal life or adulthood
caused alterations in maternal behaviour.

Researchers at University of Cincinnati report that BPA is
linked to chemotherapy resistance. The study demonstrated
that “BPA does not increase cancer cell proliferation like
DES [cancer-promoting compound called diethylstilbestrol]
does. It’s actually acting by protecting existing cancer
cells from dying in response to anti-cancer drugs, making
chemotherapy significantly less effective.”

The Canadian government announced the drafting of
regulations that will prohibit the import, sale and
advertising of polycarbonate baby bottles that contain BPA.

Based on a review by a subcommittee, the US Food and Drug
Administration (US FDA) stated that “consumers should know
that, based on all available evidence, the present
consensus among regulatory agencies in the United States,
Canada, Europe, and Japan is that current levels of
exposure to BPA through food packaging do not pose an
immediate health risk to the general population, including
infants and babies.” In addition, the US FDA thinks the
Canadian restrictions on BPA are “out of an abundance of
caution.”

January 2009. The US FDA and Health Canada’s Health
Products and Food Branch hosted a meeting of
representatives of U.S and Canadian manufacturers and users
of food packaging materials containing BPA. They discussed
what is to be done to help minimize the levels of BPA in
food. The meeting was also part of FDA’s efforts to assist
the manufacturing industry in its voluntary BPA reduction
efforts.

So what can we do to protect ourselves from BPA?

Recommendations from PEHSU – Avoid plastics with symbol # 3
(PVC or polyvinyl), symbol # 6 (PS or polystyrene foam) and
symbol #. Do not microwave food/beverages in plastic. Do
not microwave or heat plastic cling wraps. Do not place
plastics in the dishwasher. If using hard polycarbonate
plastics (water bottles/baby bottles/sippy cups), do not
use for warm/hot liquids. Use safe alternatives such as
glass or polyethylene plastic (symbol #1). Avoid canned
foods when possible (BPA may be used in can linings). Look
for labels on products that say “phthalate-free” or
“BPA-free”.

Recommendations from the Center for Science in the Public
Interest (CSPI): Avoid plastic containers made of
polycarbonate. Any bottle or container made of
polycarbonate has the recycling No. 7 on the bottom. When
possible, prepare or store food—especially hot foods
and liquids—in glass, porcelain, or stainless steel
dishes or containers. If you have polycarbonate plastic
food containers, don’t microwave them. The plastic is more
likely to break down and release BPA when it’s repeatedly
heated to high temperatures. Don’t wash polycarbonate
plastic containers in the dishwasher. The detergent may
break down the plastic, which could release BPA. Use infant
formula bottles that are made of glass or BPA-free plastic.
BornFree (newbornfree.com) is one of many companies that
make them. When you can, replace canned foods with foods
that are fresh, frozen, or packaged in aseptic
(shelf-stable) boxes. At least one manufacturer—Eden
Foods—lines its cans with a BPA alternative made from
plant extracts. A good alternative to polycarbonate is
polyethylene terephthalate (PETE), which has the recycling
No. 1 on the bottom. Avoid older versions of Delton dental
sealant…Most dental sealants are free of BPA. However,
older Delton sealants contain a compound that breaks down
into BPA, mostly during the first day after it comes into
contact with saliva.

—————————————————-
The article BPA or Bisphenol A is Everywhere – Are We Safe?
may be found in it’s entirety with references and links on
http://HealthWorldNet.com .

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Just saw this report, could vaccines be the great dead end towards finding a cure? It seems an awful lot of money has been spent and many pointing fingers..

WASHINGTON (Reuters) – A special U.S. court ruled against three families on Thursday who claimed vaccines caused their children’s autism.

The Vaccine Court Omnibus Autism Proceeding ruled against the parents of Michelle Cedillo, Colten Snyder and William Yates Hazlehurst, who had claimed that a measles, mumps and rubella vaccines had combined with other vaccine ingredients to damage the three children.

“I conclude that the petitioners have not demonstrated that they are entitled to an award on Michelle’s behalf,” Special Master George Hastings, a former tax claims expert at the Department of Justice, wrote in the Cedillo ruling.

The families sought payment under the National Vaccine Injury Compensation Program, a no-fault system that has a $2.5 billion fund built up from a 75-cent-per-dose tax on vaccines.

No judges but instead three “special masters” heard the three test cases representing thousand of other petitioners.

They asked whether a combination vaccine for measles, mumps and rubella, or MMR, plus a mercury-containing preservative called thimerosal, caused the children’s symptoms.

Read More here

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Casein Free Gluten Free Recipes

These recipes are a great resource to help adhering to a strict diet and some variation to taste can be made to the ingredients depending on what the diet requires.
TOP- Before doing anything. Please consult with your child’s healthcare provider before making any dietary changes. This information is not to be taken as medical advice.

Banana Bread

1/4 cup rice milk
6 tablespoon safflower oil
6 tablespoon pure maple syrup
2 1/4 cup mashed ripe bananas (about 5 medium bananas)
1 1/2 cups rice flour (I used 3/4 cup brown rice flour and 3/4 cup white rice flour– Blending the 2 flours give a nice consistency)
1/2 cup tapioca flour
2 tablespoon roasted grain beverage powder ( You may use rice protein instead)
1 teaspoon baking soda
1 teaspoon aluminum free baking powder
1/2 teaspoon sea salt
1 cup walnuts ( Raisins can be used for those with a nut allergy)

Preheat the oven to 350 degrees. Lightly oil a loaf pan or cake pan and dust with flour.
Put the rice milk, oil, maple syrup, and bananas in a blender and blend until smooth.
In a large bowl , whisk the flour, beverage powder (or rice protein) baking soda, baking powder, and salt until well combined.
Add banana mixture and combine, using few strokes as possible. Do not over mix.
Fold in walnuts or raisins).
Scrape into pan and smooth the top. Bake for 30-35 minutes, or until toothpick inserted into the center of the bread comes out clean.

Macaroni & Cheese
2 tablespoons butter ( You can use ghee–clarified casein free butter)
2 tablespoons flour (You can use gluten free pantry’s all-purpose baking flour mix)
1/4 teaspoon sea salt
1 cup rice milk
Dash of onion powder to taste
Butternut squash

You’ll also need gluten-free elbow macaroni noodles

Cut up butternut squash and cook by boiling in water.
While butternut squash is cooking begin basic white sauce.
Melt butter in saucepan over low heat.
Blend in flour and salt, stirring until mixture is smooth and bubbly.
Remove from heat.  Stir in the milk and onion powder; return to heat and cook, stirring constantly for about 1 minute, until thickened.
Once butternut squash is cooked. Drain it and mash it.  Then add the squash to the thick white sauce.  The more squash you add the more yellow it gets. Just keep adding until you get the color you want.
Pour the yellow sauce over cooked brown rice elbow macaroni and there you’ll have
macaroni and cheese (WITHOUT THE CHEESE!)
Pumpkin Waffles

2 eggs (Or use egg replacer or guar gum)
1 3/4 cups rice milk
3/4 cup canned pumpkin
2 tablespoons vegetable oil
2 cups gluten free pantry all purpose baking mix
2 tablespoons sugar
2 teaspoons baking powder
1/2 teaspoon cinnamon
1/4 teaspoon salt
1/4 teaspoon nutmeg

Heat waffle iron.  In blender jar combine rice milk, pumpkin, oil and eggs.  Blend at mix about 10 seconds.  Add  remaining ingredients.  Blend at mix about 60 seconds, scrape sides of blender jar every 20 seconds.   Be sure to spray the waffle iron well and bake in hot waffle iron until waffles are golden brown about 3 to 5 minutes.  May be served with maple syrup.

Portuguese Soup

Olive oil
Garlic
Onions
Stew beef (or short ribs)
Black pepper
Potatoes
1 big can Kidney beans
1 big can Cannelli beans
Carrots (optional)
Kale (can buy kale in pre cut bags)
Water (or for a really nice flavor use chicken stock)

There is no science to this soup.  Just layer each ingredient into
the pot beginning with the beef. Put desired amounts of ingredients into the pot and let everything cook down till the flavors gel together.  Soup tastes better the next day.
You can add a can of split pea soup to this same recipe for a really nice flavor (green or yellow split pea is fine).

Gluten Free White Bread
(You will need a Bread Machine to make this.  We use the Breadman and this comes out delicious–almost better than the real thing!)

2 1/2 cups white rice flour
1/2 cup potato starch flour
1/2 cup tapioca starch flour
1 Tbsp xanthan gum
1 tsp salt
2 Tbsp sugar
1 package of dry active yeast
3 large eggs (beaten)
1/4 cup sunflower oil
1 tsp cider vinegar
1/2 cup milk substitute (rice or potato milk)
3/4 cup warm water

Follow instructions of your bread machine for baking details.

Tapioca Pudding
DELICIOUS!!

3 cups Organic Coconut Milk
1/4 cup Organic Granulated Tapioca
1/8 tsp. cardamom or cinnamon
1/8 tsp. nutmeg
1/8 tsp. salt (optional)
1 tsp. vanilla extract
1/2 cup sugar

In a saucepan, simmer the ingredients (except for the vanilla and sugar).  Cook for 10 minutes, stir often until tapioca is completely transparent.  Remove from heat, add sugar and vanilla until completely blended.  Set aside to cool. Serve slightly warm or at room temperature in individual bowl.  You can top with fresh fruit such as berries or bananas.

Casein Free Ice Cream

Approx. 1 cup of Frozen Bananas
Approx. 1/2 cup coconut milk
Add any frozen or thawed fruit of choice to add more flavor
Dash of sugar (optional)
** This is a flexible recipe that is not set in stone.  You can get as creative as you like–but the key is to use frozen bananas as your ice base.

In a food processor, add bananas and blend at a low speed.  Slowly pour in coconut milk until desired texture and consistency is reached.  You can also add more frozen fruit such as strawberries.  Final result should be a thick, creamy, delicious ice cream treat!

Disclaimer: The information and postings on this site are presented for support and educational purposes only.  The information supplied on this page is believed to be reliable but its accuracy cannot be guaranteed.  UnlockAutism.com and AutismKey.com, its owner(s) and/ or webmaster(s) will not be held liable for any adverse actions or events related (directly or indirectly) to the information and/or recipes provided herein.  IN OTHER WORDS, USE THESE RECIPES AT YOUR OWN RISK AND ALWAYS CONSULT WITH YOUR CHILD’S HEALTHCARE PROVIDER!

Source – A great resource site – AutismKey.com

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The development, maintenance, and repair of myelin is the single most important factor affecting cognition and behavior, according to a UCLA neurology professor who has collected extensive data on the nerve insulator. In an article to be published in an upcoming issue of Biological Psychiatry, George Bartzokis, MD, asserts that myelin may be the universal cause or contributor to a wide range of neuropsychological brain disorders, from autism to Alzheimer’s disease. Dr. Bartzokis, who directs the UCLA Memory Disorders and Alzheimer’s Disease Clinic in Los Angeles, suggests that using noninvasive imaging technology to view the miles of myelin in the brain as it grows and breaks down throughout a human life cycle may offer insights leading to the development of new treatments for brain disorders. Nicotine, which studies have suggested enhances the growth and maintenance of myelin, could be one such novel treatment.

In some of the first research to approach brain disorders from a myelin-centered point of view, Dr. Bartzokis studied the effects of cholinergic treatments, including acetylcholinesterase inhibitors (AChEIs) that are used to improve a neuron’s synaptic signaling in people with diseases such as Alzheimer’s. Some data suggest that such treatments may even modify or slow the progression of Alzheimer’s as well as other diseases.

Nicotine, Age, and Disease

Dr. Bartzokis hypothesizes that cholinergic stimulation at neuronal synapses affects the myelination process throughout brain development in the course of a human’s lifetime.He found in clinical trials that cholinergic treatment protects brain cells, while postmortem and imaging data have shown cholinergic receptor changes during brain development and degeneration. Trials have also revealed epidemiologic evidence that nicotine from tobacco may have a protective effect on degenerative diseases of old age and younger psychiatric populations. Cholinergic treatments have also shown efficacy in the aging process and age-related neurodegenerative diseases such as Alzheimer’s disease, as well as some neurodegenerative diseases like autism and ADHD.

According to Dr. Bartzokis, myelination development resembles an inverted “U” over the course of a lifetime, with increasing myelin development peaking in middle age and breaking down and declining in later years. Following the analogy of the Internet, Dr. Bartzokis says the “connectivity” provided by myelination increases speed by 10-fold and decreases refractory time by 34-fold. Thus, myelination increases the “bandwidth,” or processing capacity, of our brain’s Internet by 340-fold and is “indispensable for developing our uniquely elaborate higher cognitive functions.”

Different cortical regions myelinate at different ages, with later-myelinating oligodendrocytes growing increasingly more complex as we age. Irregular development during the most complex stages of the myelination process contributes to several of the neuropsychiatric disorders that tend to manifest in the early years. These disorders—eg, autism, ADHD, schizophrenia, mood disorders, addictions—are defined by overlapping cognitive and behavioral symptom clusters.

According to Dr. Bartzokis, healthy individuals with normal myelin development typically lose 45% of their myelinated fiber length when they reach the degeneration phase in adulthood. This change in the brain may cause progressive losses of memory and cognitive functions, as well as mild to severe behavioral changes.

The loss of myelin and its components such as sulfatide, myelin basic protein, and cholesterol begins early in the development of Alzheimer’s disease, well before diagnosis of dementia or mild cognitive impairment. The myelin breakdown process is further modified by risk factors such as the presence of APOE ε4 or environmental factors such as a head trauma.

Nicotine’s Effect on Myelination and Repair

Recent research has unveiled some surprising findings on the influence of nicotine on myelination and the aging process. Direct nicotinic stimulation associated with smoking has been shown to increase nicotinic receptors in the late myelinating frontal and temporal intracortical regions. Unlike most agonists, nicotine causes an up-regulation of its receptors and has been shown to accelerate brain function recovery when white matter is damaged.

Nicotine dependence is common among people with psychiatric disorders. Some researchers have suggested the high prevalence of nicotine use among the psychiatric population represents an unconscious effort to “self-medicate.” Research on proteins has suggested that nicotine may marginally increase the expression of myelin proteins; other addictive drugs (eg, cocaine, alcohol) along with developmental diseases (eg, schizophrenia, bipolar disorder, depression) show a decrease of these proteins.

Other research has found an association between nicotinic stimulation and protective effects in schizophrenia and autism, where cortical myelination deficits have been documented. While nicotine has well-known negative effects on overall health, smoking during later years is also associated with a reduced likelihood of the development of degenerative conditions like Alzheimer’s and Parkinson’s diseases. Using the myelin-centered model, the apparent beneficial aspects of smoking on brain disorders can be attributed to nicotine’s stimulation of oligodendrocyte precursors. Dr. Bartzokis believes that nicotine, delivered through a patch, not through smoking cigarettes, should be studied for its efficacy in promoting the growth and maintenance of myelin, and that AChEIs “deserve much closer scrutiny” as a therapy for the prevention of both developmental and degenerative brain disorders.

—Kathlyn Stone http://www.neuropsychiatryreviews.com/07jan/myelin.html

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Wanted to repost this article we shared afew months back. I was shocked that the baby formula I was ent home with from the hospital and provided by Similiac used PVC and was stamped with code #3. Why are we still using this stuff?

It’s worth avoiding all plastics if you can. You can identify a plastic by looking at the recycling code number that appears inside a triangle at the bottom of many containers.

Resin code #3 – Polyvinyl chloride (PVC) can leach phthalates, known male reproductive toxicants. It can be identified by code 3. One way to avoid it in the kitchen is by choosing plastic wrap made from polyethylene rather than PVC. If a box is not labeled, find a brand that is or call the manufacturer.

Resin code #6 – Polystyrene is used in Styrofoam products. It may leach styrene (a neurotoxin) when it comes into contact with hot, acidic, or fatty foods. It’s marked with recycling code 6.

Resin code #7 – Polycarbonate can leach bisphenol-A (BPA), an endocrine disruptor associated with a long list of health concerns. Baby bottles, “sippy” cups, 5-gallon water jugs, and reusable beverage bottles are typically made out of this plastic. Products may be marked with recycling code 7 (also includes any plastic that doesn’t fit into the 1 to 6 recycling code categories) and/or the letters “PC.”

The following plastics are considered safest for food storage. Glass and stainless steel are the best options as they do not have pores and bacteria catching scratches.

Resin code #1 – Polyethylene terephthalate ethylene (PETE), code 1.

Resin code #2 – High-density polyethylene (HDPE), code 2.

Resin code #4 – Low-density polyethylene (LDPE), code 4.

Resin code #5 – Polypropylene (PP), code 5.

Useful tips for when you do use plastic..

* Don’t microwave food plastic containers. HEat creates a good environment for chemicals to be re-activated and to leach out when plastic is heated. “Microwaveable plastic” doesn’t guarantee anything. Cover foods in the microwave with wax paper or a plate. If you do use plastic wrap, then make sure it doesn’t touch the food.

* Avoid putting hot foods in plastic containers. Let leftovers cool off before storing them in plastic.

* Take good care of plastics by not washing them with harsh chemicals, and dispose of scratched and worn containers. Just as your vet suggests no plastic bowls for your pets, we should follow the same advice.

Not sure about you, but i dont recall seeing plastic bottles around when I was a kid, it was glass and that was it. Now with nearly every child drinking form plastic and then followed up with nearly every adult drinking form a Poland Spring plastic water botle, its no wonder we are all poisopning ourselves! Use glass or stainless steel, avoid plastic!

For more green tips, visit Green and Ready

We use a product called BornFree made of “Glasstic” out of canada, one of the first PBA free plastic products on the market, but I would still prefer a glass baba for my kid. Here is a link to Consumer Reports story on this subject

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You may recall seeing the Eye Chart last time you visited the doctor. Today it is also common to see the entire human body chart, inner ear chart, neck, back and knee joint models and other props for the doctor to use with patients when explaining our all too common ailments.

With the explosive growth of Autism rates, can we expect to see more of this chart appearing in a pediatricians office near you?

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During the 3rd Presidential Debate, held at Hofstra University recently, both candidates spoke about autism. In response to a question from CBS News’ Bob Schieffer, “why would the country be better off if your running mate became president” the senators made the following remarks:

Sen. McCain: …She (Sarah Palin) also understands special needs families. She understands that autism is on the rise. We’ve got to find out what’s causing it and we’ve got to reach out to these families and help them and give them the help they need as they raise these very special needs children. She understands that better than almost any American that I know. I’m proud of her.

Sen. Obama: …I think it’s very commendable the work she (Sarah Palin) has done on behalf of special needs. I agree with that John. I do just want to point out that autism for example or other special needs will require some additional funding if we’re going to get serious in terms of research. That is something that every family that advocates on behalf of disabled children talks about. And if we have an across the board spending freeze we’re not going to be able to do it.

In response to the Bob Schieffer’s question “Do you think the federal government should play a larger role in the schools and I mean federal money?” the senators made the following remarks:

Sen. Obama: I do think it is important for the federal government to step up and help local school districts do the things they need to do….We did the right thing by saying every school should provide education for children with special needs but we never followed through on the promise of funding, and that left local school districts very cash strapped.

Sen. McCain: In town hall meeting after town hall meeting, parents come with kids, children, precious children who have autism. Sarah Palin knows about that better than most. And we’ll find, and we’ll spend the money on research to find the cause of autism, and we’ll care for these young children and all Americans will open their wallets and their hearts to do so.

We finally may have some real representation in the government with either candidate.  Palin knows the pain personally, Obama seems to understand  the need for federal funding of local schools. Should be interesting how this plays out, lets keep the Special Needs topic front and center.

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Dear Friends:

The Third Annual Rockland County Autism Symposium will be held on September 25, 2008 at the Holiday Inn Hotel in Suffern, NY. Once again, I am pleased to co-sponsor this symposium with Camp Venture, Inc., the Needelman Family and Mindworks, a private foundation.

We are again privileged to feature presenters from prestigious institutions, who are dedicated and distinguished experts in the field of Autism Spectrum Disorders. Our focus this year will be on new research, abnormalities in sleep, pharmacological treatment, a look at adults with Autism and more. You may view the full program and information on our speakers, above.

Last year, our Symposium set the Rockland County record for attendance at any symposium to date. We look forward to this year’s event with great anticipation, and your attendance and participation is both valued and appreciated. Through the generosity of the Needelman Family and Mindworks there is no fee for registration and a complimentary lunch will be provided. To secure a seat, please click the reservation link and do it soon! Last year, we reached maximum capacity well in advance of the event. Please feel free to pass this information onto others interested in Autism.

I look forward to seeing you at this event on September 25th.

Sincerely,

John Murphy
Rockland County Legislator
President, Camp Venture, Inc. Board of Directors

Here is a short fundraiser video on the Camp Venture Equestrian Therapy program.

2008 Autism Symposium
Holiday Inn Holidome & Conference Center
3 Executive Boulevard
Suffern, NY 10901
Thursday, September 25, 2008
8:00 AM – 4:00 PM
Admission:Free for pre-registrants
$25.00 for walk-in and late registrants
Contact: Betsy Saetre
(845) 638-5184

or visit http://www.rocklandautismsymposium.com/

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This is the idiot who caused millions of dollars and years of research to go to waste. All this for 55,000 British Pound Sterling. Where are is the tar and feathers?  What has Elsevier done to make it up to all of our children ? How about $100 million in Autism funding ?

The editor of the Lancet said last night that the scientific paper which sparked the row about the safety of the MMR vaccine would not have been published if senior staff had been aware that its lead author had not revealed “a serious conflict of interest”.

Richard Horton said that Andrew Wakefield, the doctor whose research suggested a link between the triple jab against measles, mumps and rubella and autism, had made “an important error of judgement” in failing to say he had received an alleged £55,000 from the Legal Aid Board, now the Legal Services Commission to investigate grounds for legal action by parents of allegedly vaccine-damaged children.

Dr Wakefield’s article, published in the medical journal six years ago, caused a drop in uptake of the MMR vaccine and protracted argument. It also made the author a pariah in the eyes of the medical establishment.

Two months ago senior doctors boycotted a televised debate on the vaccine, scheduled to run after a Channel 5 drama documentary about Dr Wakefield’s work, as they regarded it as biased and emotive.

Dr Wakefield, who worked at the Royal Free Hospital, in north London, when the paper was published, denied last night that the authors of the report had any knowledge that one child investigated for the study reported in the Lancet had a legal aid certificate at the time.

Investigations as a result of allegations made to the Lancet in the past few days suggest that as many as four of the 12 reported cases may have been on a list of 10 children on whom Dr Wakefield was commissioned by a solicitor to make studies. The exact number has still to be confirmed.

The two studies were completely separate and money from the Legal Aid Board was paid into a special research account administered by the hospital trust.

Dr Wakefield said: “Whether parents perceived an association with MMR vaccine or not, whether parents had approached lawyers with an intent to seek legal redress, or whether children were in receipt of legal funding or not, had no bearing whatsoever on their selection for clinical investigation of inclusion in the Lancet report.”

The paper in fact did not claim to prove a link between the MMR vaccination and autism, although Dr Wakefield said at its launch that he thought parents might be advised to give the jabs separately.

Mr Horton refused to reveal last night who had made six serious allegations of research misconduct. Three were not accepted.

“We regret that aspects of funding for parallel and related work and the existence of ongoing litigation that had been known during clinical evaluation of the children reported in the 1998 Lancet paper were not disclosed to editors.

“We judge that all this information would have been material to our decision-making about the paper’s suitability, credibility and validity for publication.”

The Lancet would publish an editorial commentary and statements from researchers involved in the 1998 study “as soon as possible”.

Mr Horton underlined how seriously he viewed the case. “In my view, not to disclose such a serious conflict of interest was an important error of judgement and conflicted with our guidelines on conflict of interest at the time.

“It is always very difficult with hindsight, but if we had known Dr Wakefield was not only lead investigator in the Lancet paper but also had been commissioned by the Legal Advisory Board, I am sure our view would have been this was a fatal conflict of interest and we would not have published the paper.”

Dr Wakefield’s co-authors have become increasingly critical, saying they believe in the safety of the MMR. Dr Simon Murch and colleagues have continued to research links between inflammation of the gut and autism and believe there is evidence of an association.

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